Novo Nordisk

About the Department

At Novo Nordisk, we want to make a difference. For more than 100 years, we have led the way in diabetes care. Being part of Novo Nordisk allows our employees to embark on life-changing careers, and the opportunity to help improve the quality of life for millions of people around the world.

Our Bloomington, Indiana site is a state-of-the-art facility where we have an integrated model from process and formulation to clinical and commercial biomanufacturing and drug product fill/finish and packaging. The Bloomington campus is a recognized facility where talented teams work with innovators to help develop, manufacture and supply products to patients around the world.

What we offer you:

1. Leading pay and annual performance bonus for all positions
2. All employees enjoy generous paid time off including 14 paid holidays
3. Health Insurance, Dental Insurance, Vision Insurance – effective day one
4. Guaranteed 8% 401K contribution plus individual company match option
5. Family Focused Benefits including 14 weeks paid parental & 6 weeks paid family medical leave
6. Free access to Novo Nordisk-marketed pharmaceutical products
7. Tuition Assistance
8. Life & Disability Insurance
9. Employee Referral Awards

At Novo Nordisk, you will find opportunities, resources, and mentorship to help grow and build your career. Are you ready to realize your potential? Join Team Novo Nordisk and help us make what matters.

The Position

This position requires a variety of skills necessary for biotech company operations. The position is an entry level laboratory role with the expectation that the candidate can be trained on technical procedures and once trained, execute them consistently and reliably. Additionally, this position may support preventative maintenance and basic laboratory maintenance activities while maintaining a GMP quality system.

Schedule: 2nd shift: Monday - Friday 2:30pm-11:00pm

Relationships

Reports to: Supervisor, QC

Reports to Supervisor or above.

Essential Functions

• Performs general lab housekeeping in adherence to 5S standards including cleaning/sterilizing of lab and lab materials, disposal of trash and recyclables, autoclaving, ordering, and stocking supplies
• Stages materials/components for use within cGMP Quality Control lab
• Accurately completes routine and preventive maintenance on simple equipment
• Perform facility monitoring of gas and water sampling
• Perform routine environmental monitoring in manufacturing environment: active air sampling, non-viable particulate monitoring, surface and personnel sampling
• Log in samples into laboratory tracking software
• Actively participates in team meetings and/or training sessions
• Other duties as assigned

Physical Requirements

Frequent sitting, standing, walking, reading of written documents and use of computer monitor screen, reaching with hands and arms, talking, writing, listening. Occasional stooping, kneeling, crouching, bending, carrying, grasping. Frequent lifting and/or moving up to 10 pounds and occasional lifting and/or moving up to 50 pounds. Must comply with EHS responsibilities for the position. Working conditions will be Heating Ventilation and Air Condition controlled. Working in a lab environment will require working with skin irritants, lung irritants, electrical equipment, sharp instruments, toxic materials, and hazardous waste. Safety procedures will be followed to minimize exposure, including clean room gowning.

Qualifications

• High School Diploma required with typically 0-2 years of industry experience preferred
• Technical Certificate or higher preferred
• Must be able to read and understand English-written job instructions and safety requirements
• Preferred:
  • Familiarity with clean room procedure, aseptic technique, and general lab equipment experience
  • cGMP, Good Documentation Practices (GDP), or Good Laboratory Practices (GLP) knowledge
  • Experience following standard operating procedures (SOP)
  • General laboratory equipment experience, including micropipettes
  • Maintain high quality laboratory documentation in accordance with applicable regulatory guidance and Site SOPs
• Ability to learn and retain technical information
• Proactively address work issues at an individual level
• Executes assigned laboratory activities and methods with minimal guidance
• Ability to follow a variety of instructions furnished in written, oral, diagram, or schedule form. Proactively seek information to fill gaps in knowledge base
• Mathematical and scientific reasoning ability
• Learning core techniques such as pipetting and buffer preparation techniques
• Ability to work effectively under accelerated timelines to meet multiple deadlines
• Well organized with ability to handle and direct multiple activities simultaneously
• Ability to see and hear, read, and write clear English
• Requires adaptability, analysing, assessing, calculating, decision making, dependability, good judgment, reading, memorizing, social skills, speaking, stress control, writing
• Ability to communicate effectively and follow/retain detailed written and verbal instruction in an accurate, timely, safe, and professional manner with supervisor, group members, and other departments as necessary, in a professional and accurate manner
• Ability to manage time effectively to complete assignments in expected time frame and independently seek out additional work when tasks are completed ahead of time
• Ability to cooperate with coworkers within an organized team environment or work alone
• Detail oriented with ability to work effectively under high pressure with multiple deadlines
• Strong ability to multi-task in a fast-paced environment
• Positive attitude and ability to work with others
• Ability to put aside personal opinions and focus on business needs, department needs, or group needs
• Lead by example according to Catalent's values and culture
• Fast paced
• Performance driven
• Customer focused
• Collaborative and inclusive
• Team player

We commit to an inclusive recruitment process and equality of opportunity for all our job applicants.

At Novo Nordisk we recognize that it is no longer good enough to aspire to be the best company in the world. We need to aspire to be the best company for the world and we know that this is only possible with talented employees with diverse perspectives, backgrounds and cultures. We are therefore committed to creating an inclusive culture that celebrates the diversity of our employees, the patients we serve and communities we operate in. Together, we’re life changing.

Novo Nordisk is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, ethnicity, color, religion, sex, gender identity, sexual orientation, national origin, disability, protected veteran status or any other characteristic protected by local, state or federal laws, rules or regulations.

If you are interested in applying to Novo Nordisk and need special assistance or an accommodation to apply, please call us at 1-855-411-5290. This contact is for accommodation requests only and cannot be used to inquire about the status of applications.